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Volumn 53, Issue 15, 2014, Pages 3913-3916

Enantioselective N-H insertion reaction of α-aryl α-diazoketones: An efficient route to chiral α-aminoketones

Author keywords

asymmetric catalysis; carbenes; chiral proton shuttle; chiral aminoketones; diazo compounds

Indexed keywords

CARBOXYLATION; CATALYSIS; PHOSPHORIC ACID; REACTION RATES; SYNTHESIS (CHEMICAL);

EID: 84897990229     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201400236     Document Type: Article
Times cited : (117)

References (64)
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    • An N-H insertion of α-diazoketones catalyzed by a chiral iron porphyrin was investigated; however, no chiral induction was obtained.
    • An N-H insertion of α-diazoketones catalyzed by a chiral iron porphyrin was investigated; however, no chiral induction was obtained., I. Nicolas, T. Roisnel, P. L. Maux, G. Simonneaux, Tetrahedron Lett. 2009, 50, 5149-5151.
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    • The diazoketones were prepared according to reported procedures:, and ref. [4j].
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    • The absolute configuration of 5 a was determined by comparison to reported values.
    • The absolute configuration of 5 a was determined by comparison to reported values:, Y. Qin, C.-H. Wang, Z.-Y. Huang, X. Xiao, Y.-Z. Jiang, J. Org. Chem. 2004, 69, 8533-8536.
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    • CCDC 980485 (5 b) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.